Drakesmith Mark, Dutt Anirban, Fonville Leon, Zammit Stanley, Reichenberg Abraham, Evans C John, McGuire Philip, Lewis Glyn, Jones Derek K, David Anthony S
Cardiff University Brain Research Imaging Centre (CUBRIC), School of Psychology, Cardiff University, Manidy Road, Cardiff CF24 4HQ, UK; Neuroscience and Mental Health Research Institute (NMHRI), School of Medicine, Cardiff University, Maindy Road, Cardiff CF24 4HQ, UK.
Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, DeCrespigny Park, London SE5 8AF, UK.
Neuroimage Clin. 2016 Sep 4;12:550-558. doi: 10.1016/j.nicl.2016.09.002. eCollection 2016.
Grey matter (GM) abnormalities are robust features of schizophrenia and of people at ultra high-risk for psychosis. However the extent to which neuroanatomical alterations are evident in non-clinical subjects with isolated psychotic experiences is less clear.
Individuals (mean age 20 years) with (n = 123) or without (n = 125) psychotic experiences (PEs) were identified from a population-based cohort. All underwent T1-weighted structural, diffusion and quantitative T1 relaxometry MRI, to characterise GM macrostructure, microstructure and myelination respectively. Differences in quantitative GM structure were assessed using voxel-based morphometry (VBM). Binary and ordinal models of PEs were tested. Correlations between socioeconomic and other risk factors for psychosis with cortical GM measures were also computed.
GM volume in the left supra-marginal gyrus was reduced in individuals with PEs relative to those with no PEs. The greater the severity of PEs, the greater the reduction in T1 relaxation rate (R1) across left temporoparietal and right pre-frontal cortices. In these regions, R1 was positively correlated with maternal education and inversely correlated with general psychopathology.
PEs in non-clinical subjects were associated with regional reductions in grey-matter volume reduction and T1 relaxation rate. The alterations in T1 relaxation rate were also linked to the level of general psychopathology. Follow up of these subjects should clarify whether these alterations predict the later development of an ultra high-risk state or a psychotic disorder.
灰质(GM)异常是精神分裂症以及精神病超高风险人群的显著特征。然而,在仅有精神病性体验的非临床受试者中,神经解剖学改变的明显程度尚不清楚。
从一个基于人群的队列中识别出有(n = 123)或无(n = 125)精神病性体验(PEs)的个体(平均年龄20岁)。所有人均接受了T1加权结构成像、扩散成像和定量T1弛豫测量MRI,以分别表征GM的宏观结构、微观结构和髓鞘形成。使用基于体素的形态计量学(VBM)评估GM定量结构的差异。测试了PEs的二元和有序模型。还计算了社会经济因素和其他精神病风险因素与皮质GM测量值之间的相关性。
与无PEs的个体相比,有PEs的个体左缘上回的GM体积减小。PEs的严重程度越高,左颞顶叶和右前额叶皮质的T1弛豫率(R1)降低幅度越大。在这些区域,R1与母亲教育程度呈正相关,与一般精神病理学呈负相关。
非临床受试者中的PEs与灰质体积减少和T1弛豫率的区域降低有关。T1弛豫率的改变也与一般精神病理学水平相关。对这些受试者的随访应能阐明这些改变是否预示着超高风险状态或精神病性障碍的后期发展。